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Most Recent Evidence Behind Aggregometry and Genotyping Methods as Platelet Function Testing for Tailored
Sylwia N Gajda1, Łukasz Kołtowski1, Mariusz Tomaniak1
11st Department of Cardiology, Public Central Teaching Hospital, Warszawa, Poland.
Insights
Platelet function testing, including aggregometry and genotyping, helps manage antiplatelet therapy for high-risk cardiac patients. Personalizing treatment based on these tests can reduce ischemic events and improve patient outcomes.
Area of Science:
- Cardiology
- Pharmacogenomics
- Clinical Chemistry
Background:
- Optimal platelet reactivity (PR) is crucial for patients undergoing invasive cardiac procedures.
- Individual responses to clopidogrel vary significantly, leading to poor responders (5-44%) and increased ischemic event risk.
- Newer antiplatelet agents like prasugrel and ticagrelor have risks of increased bleeding.
Purpose of the Study:
- To review the latest evidence on platelet function testing methods.
- To evaluate the clinical utility of aggregometry and genotyping in managing antiplatelet therapy.
- To determine the best approach for identifying high-risk patients and personalizing antiplatelet treatment.
Main Methods:
- Review of recent evidence on aggregometry and genotyping for platelet function testing.
- Analysis of clinical trials and meta-analyses assessing the impact of these tests on patient outcomes.
- Examination of the genetic correlation between CYP2C19 gene variants and clopidogrel response.
Main Results:
- Aggregometry demonstrated benefit in 5 trials and 1 meta-analysis.
- Genotyping showed a positive clinical effect in 10 studies.
- CYP2C19*2 allele carriers exhibit higher PR, increasing thrombotic event risk.
Conclusions:
- Platelet function testing, through aggregometry and genotyping, is beneficial for high-risk cardiac patients.
- Personalized antiplatelet therapy, guided by these tests, can decrease adverse ischemic outcomes.
- Combining aggregometry and genotyping may offer the most effective strategy for identifying high-risk individuals.
Abstract:
Aggregometry and genotyping are methods of platelet function testing, which can be beneficial for high-risk patients undergoing invasive cardiac procedures. An optimal level of platelet reactivity (PR) should be maintained. There are discrepancies between individuals and their response to clopidogrel, accounting for the incidence of poor responders from 5% to 44%. This phenomenon predisposes the patients to increased risk of ischaemic events and thereby overall poorer clinical outcome. Prasugrel and tricagrelor are newer without genetic correlation to their action, however associated with increased bleeding risk. Aggregometry methods assess platelet reactivity at the exact moment of blood sampling. They reflect "phenotype" of the patient and vary after drug administration or dose change. The most popular tests are Light Transmission Aggregometry, Vasodilator-Stimulated Protein, VerifyNow, Multiple Electrode Aggregometry and Thrombelastography. There is proven genetic correlation between some cytochrome enzymes on clopidogrel response. The most widely tested is gene CYP2C19, which produces the enzyme transforming clopidogrel into an active metabolite. The CYP2C19*2 allele carriers have higher PR which can result in more thrombotic events. The manuscript shows the most recent evidence behind platelet function testing. Aggregometry is shown to be beneficial in 5 trials and 1 meta-analysis, while one paper was of different opinion. Ten studies show a positive clinical effect of genotyping on patients' outcome, while one does not support it. The best method of identifying high-risk individuals could be both methods and personalisation of antiplatelet therapy may decrease adverse ischaemic outcomes.
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